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SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening Option

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250650
510(k) Type
Traditional
Applicant
Arineta , Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/15/2025
Days to Decision
42 days
Submission Type
Summary

SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening Option

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250650
510(k) Type
Traditional
Applicant
Arineta , Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/15/2025
Days to Decision
42 days
Submission Type
Summary